BEUDAMED
    FDA Adverse Event Summary report: N

    THE BRIDGE EAR DEVICE FOR OPIOD WITHDRAWAL

    MDR report key: 7352342 · Received March 19, 2018

    Report

    Report Number
    MW5075971
    Date Received
    March 19, 2018
    Date of Event
    February 20, 2018
    Report Date
    March 17, 2018
    Manufacturer
    UNK
    Product Code
    BWK
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT GIVEN THE "BRIDGE DEVICE" FOR OPIOID WITHDRAWAL WITH NO EVIDENCE OF EFFICACY, AND THEN LEFT REAL TREATMENT DUE TO "I HAVE THE BRIDGE."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    194062 THE BRIDGE EAR DEVICE FOR OPIOD WITHDRAWAL STIMULATOR, ELECTRO-ACUPUNCTURE BWK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 39 YR Other